Selective synthesis and structural elucidation of S-acyl- and N-acylcysteines

Alan R. Katritzky, Srinivasa R. Tala, Nader E. Abo-Dya, Kapil Gyanda, Bahaa El Dien M El-Gendy, Zakaria K. Abdel-Samii, Peter J. Steel

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30 Scopus citations

Abstract

(Chemical Equation Presented) N-(Acyl)-1H-benzotriazoles 6a-f react with L-cysteine 5 at 20°C to give exclusively (i) N-acyl-L-cysteines 8a-e in the presence of triethylamine in CH3CN-H2O (3:1), but (ii) S-acyl-L-cysteines 7a-e in CH3CN-H2O (5:1) in the absence of base. Structures 7b, 7d and 8b, 8d are supported by 2D NMR spectroscopic methods including gDQCOSY, gHMQC, gHMBC, and 1H-15N CIGAR-gHMBC experiments. The structure of compound 8d was also supported by single-crystal X-ray diffraction.

Original languageEnglish (US)
Pages (from-to)7165-7167
Number of pages3
JournalJournal of Organic Chemistry
Volume74
Issue number18
DOIs
StatePublished - Sep 18 2009

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    Katritzky, A. R., Tala, S. R., Abo-Dya, N. E., Gyanda, K., El-Gendy, B. E. D. M., Abdel-Samii, Z. K., & Steel, P. J. (2009). Selective synthesis and structural elucidation of S-acyl- and N-acylcysteines. Journal of Organic Chemistry, 74(18), 7165-7167. https://doi.org/10.1021/jo900853s